Remote Adverse Event & Product Reporting Specialist

ACTalent; EE. UU.; A distancia; USD 28.000 - 40.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Time Off / PTO

Descripción de la vacante

Actalent is seeking an Adverse Event and Product Complaint Reporting Specialist to manage AE and product complaint reporting using a patient management system, ensuring accuracy through quality checks and collaboration with clinicians.

You will perform data entry, coordinate with biopharma clients, and support clinical auditors by identifying trends and ensuring timely, compliant reporting.

Formación

• Bachelor's degree or commensurate experience preferred.
• Pharmacy technician or other clinical experience preferred.
• Oncology experience is a plus.
• Comfort working with patient management systems and clinical documentation.
• Ability to support clinical auditors by recognizing trends and issues in adverse event reporting.

Responsabilidades

• Create and submit adverse event and product complaint reports using data documented in the patient management system.
• Conduct thorough quality checks of all reports, including verifying spelling, drug manufacturer information, and grammar within clinical notes.
• Communicate with clinicians to address questions or concerns about reporting content or quality.
• Identify missing adverse events and product complaints through daily quality control processes and report findings to clinicians.
• Maintain and submit weekly and monthly reconciliation reports to biopharma clients per contract.

Conocimientos

Excel

Data entry

Attention to detail

Time management

Communication

Cross-functional collaboration

Multitasking

Healthcare experience

Customer service

Typing

Educación

Bachelor's degree or commensurate experience

Herramientas

Excel

Descripción del empleo

Actalent is seeking an Adverse Event and Product Complaint Reporting Specialist to manage AE and product complaint reporting using a patient management system, ensuring accuracy through quality checks and collaboration with clinicians.

You will perform data entry, coordinate with biopharma clients, and support clinical auditors by identifying trends and ensuring timely, compliant reporting.